rs150911354

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs150911354(C;T)

Make rs150911354(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64747224

Gene	PYGM, RASGRP2

is a	snp
is	mentioned by
dbSNP	rs150911354
dbSNP (classic)	rs150911354
ClinGen	rs150911354
ebi	rs150911354
HLI	rs150911354
Exac	rs150911354
Gnomad	rs150911354
Varsome	rs150911354
LitVar	rs150911354
Map	rs150911354
PheGenI	rs150911354
Biobank	rs150911354
1000 genomes	rs150911354
hgdp	rs150911354
ensembl	rs150911354
geneview	rs150911354
scholar	rs150911354
google	rs150911354
pharmgkb	rs150911354
gwascentral	rs150911354
openSNP	rs150911354
23andMe	rs150911354
SNPshot	rs150911354
SNPdbe	rs150911354
MSV3d	rs150911354
GWAS Ctlg	rs150911354

Max Magnitude

0

ClinVar
Risk	rs150911354(T;T)
Alt	rs150911354(T;T)
Reference	Rs150911354(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PYGM RASGRP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.64514696C>T
CLNSRC
CLNACC	RCV000493384.1,